Active substanceBotulinum neurotoxin type ABotulinum neurotoxin type A
Similar drugsTo uncover
  • Xeomin
    lyophilizate w / m 
  • Lantox
    lyophilizate for injections 
    NIKE-MED, LLC     Russia
  • Dosage form: & nbsplyophilizate for solution for injection
    Composition:

    On 1 bottle:

    botulinum toxin type A - 50 or 100 ED, gelatin - 5 mg, dextran - 25 mg, sucrose - 25 mg.

    Description:

    Powder of white color, without taste and odor, without foreign inclusions.

    Pharmacotherapeutic group:MIBP
    ATX: & nbsp

    M.03.A.X.01   Botulinum toxin

    Pharmacodynamics:

    Lantox is a sterile, lyophilized form of purified botulinum toxin type A, obtained from the culture medium of bacteria Clostridium botulinum, containing trypticase and yeast extracts.

    A botulinum toxin type A molecule consists of heavy disulfide bridges (with a molecular weight of 100,000 daltons) and light (with a molecular weight of 50,000 daltons) chains. The heavy chain has a high affinity for binding to specific receptors located on the surface of target neurons. The light chain possesses Zn2+-dependent protease activity specific for the cytoplasmic regions of the synaptosomal-binding protein having a molecular weight of 25,000 daltons (SNAP-25) and involved in the processes of exocytosis.

    First step the action of botulinum toxin type A is the specific binding of the molecule to the presynaptic membrane. This process takes 30 minutes. Second phase - internalization of the bound toxin to the cytosol through endocytosis. After internalization, the light chain acts like Zn2+-dependent protease of the cytosol, selectively cleaving SNAP-25, which in the third stage results in blockade of the release of acetylcholine from the presynaptic endings of the cholinergic neurons. The final effect This process is stable chemodenervation. Clinical manifestation of chemodenervation of cholinergic terminals is relaxation of the injected muscle or blockage of the function of exocrine glands in the injection zone.

    Pharmacokinetics:

    The duration of the clinical effect is 16-20 weeks. 10-30 days after the injection, the process of development of new axonal processes begins, which form new functionally active neuromuscular synapses, which leads to the restoration of muscle contractions.

    With intramuscular injection of botulinum toxin type A, two effects develop: direct inhibition of extrafusal muscle fibers by inhibiting alpha motor neurons at the level ofneuromuscular synapse and inhibition of muscular spindle activity by inhibiting the gamma motor neuron cholinergic synapse on the intrafusal fiber. Reduction of gamma activity leads to relaxation of the spinal cord's intrafusal fibers and reduces activity la-afferents. This leads to a decrease in the activity of both muscle stretch receptors and the efferent activity of alpha and gamma motor neurons. Clinically, this manifests itself in the pronounced relaxation of the injected muscles and a significant reduction in pain in them. Along with the process of denervation in these muscles, the process of reinnervation proceeds by the appearance of lateral processes of nerve endings, which leads to the restoration of muscle contractions 3-6 months after injection. With this in some cases, the expediency of repeated injections after 2 months is associated.

    When administered at therapeutic doses, Lantox does not penetrate the blood-brain barrier. It is excreted by the kidneys in the form of non-toxic metabolites.

    Indications:

    I. Local muscular spasms:

    - Blepharospasm;

    - Spasticity of the muscles of the upper limb: a) in the region of the hand, b) in the elbow joint region, c) in the shoulder region;

    - Spasticity of the muscles of the lower limb: a) in the region of the foot, b) in the region of the knee, c) in the region of the thigh;

    - Hemifacial spasm;

    - Hyperactive bladder;

    - Detruzor-sphincter dissynergy;

    - Hyperfunctional facial wrinkles, neurocosmetic defects;

    - Strabismus.

    II. Vegetative disorders:

    - Hyperhidrosis.

    III. Pain Syndromes:

    - Myofascial pain syndromes;

    - Chronic headaches.
    Contraindications:

    Hypersensitivity to the components of the drug.

    Violations of the neuromuscular transmission (myasthenia gravis, Lambert-Eaton syndrome, etc.)

    Pregnancy and lactation.

    Hemophilia.

    Inflammatory process at the site of injection and skin disease.

    Limitations:

    The drug is not administered at elevated temperature and acute infectious and non-infectious diseases.

    The drug is ineffective or ineffective in strabismus in 50 prism dioptres or resistant strabismus, strabismus in Down's syndrome caused by weakness of the lateral rectus muscle (lateral erectus), strabismus as a result of excessive operative correction, chronic paralytic strabismus, chronic paralysis of the VI or IV craniocerebral nerve.

    In the treatment of local muscle spasms, the drug is ineffective with fixed contractures.

    Exclusion of the drug during the period of antibiotic-aminoglycoside, erythromycin, tetracycline, polymyxin, curare-like muscle relaxants.

    Dosing and Administration:

    Local muscular spasms

    Blepharospasm

    During the injection, the patient is in a sitting position, the back of the head is propped against a fixed support. The drug is injected shallowly into the m. Orbicularis oculi, the closer to the eye, the more superficial (intradermal) in 4-5 points. At a typical blepharospasm in 2 points of the upper eyelid, located medial and lateral from the vertical pupillary line, and 2-3 points in the area of ​​the outer corner of the eye. In the course of the pretarsal blepharospasm, injection points in the upper eyelid area are located in the lower part of the upper eyelid directly near the line of eyelash growth.

    Avoid injection in the middle of the upper eyelid and the inner corner of the eye because of the risk of side effects (ptosis, lacrimation, diplopia).

    The total dose for bilateral blepharospasm in most cases is 25 units per eye. In the case of unilateral blepharospasm, injections are performed only on the side of the affected eye.The initial dose for each point is 2.0-3.0 units. The maximum dose for each point is 5.0 units. With pretarsal blepharospasm, at every point of the upper eyelid, no more than 2.0-2.5 units of ED are injected, in the region of the outer corner of the eye - according to the usual scheme.

    Use insulin syringes with non-removable needles measuring 29-33G.

    After injection for 5 minutes it is recommended to cool the area of ​​injections (near the outer eye) with bags of ice cubes. For a more rapid and persistent onset of the drug, the patient is recommended to actively shut his eyes and open his eyes within 15-20 minutes. Repeated injections are carried out as needed, but not earlier than 2 months.

    Gemifacial spasm

    The treatment of hemifacial spasm by Lantox is generally similar to the treatment of blepharospasm. The dose of Lantox with an injection only around the eye does not exceed 25 units per side.

    In the muscles of the corner of the mouth (large and small zygomatic muscles) inject 2.5 LTU of Lantox; an increase in the dose may be complicated by lowering the angle of the mouth. To maintain the symmetry of the mouth, it is possible to correct the injection into these muscles from the opposite ("healthy") side. In the prevalent variants of hemifacial spasm with the involvement of the frontal muscle, the muscles of the brow frown and platysm are additionally introduced into each muscle by 5-10 units.

    The total dose of Lantox in the prevalent variants of hemifacial spasm per procedure is 50 units or more. The maximum dose is determined individually and is the sum of the doses for each muscle involved.

    Use insulin syringes with non-removable needles measuring 29-33G. Repeated injections are carried out as needed, but not earlier than 2 months.

    Spasticity of the muscles of the upper limb

    Spasticity in the area of ​​the hand

    During the injection, the patient is in a sitting position on the stool or lying on his back, the hand lies on the horizontal plane.

    The average therapeutic dose of Lantox with abnormal flexural settings of the hand and fingers is 150 units. The total dose is divided between m. Flexor carpi radialis - 20-40 units, m. Flexor carpi ulnaris - 20-40 units, t. Flexor digitorum superficialis 20-40 units, m. Flexor digitorum profundus - 30-60 units.

    For injections use insulin syringes with non-removable needles of size 29-33G, as well as needles for intramuscular injections of size 21-23G and EMG control. Repeated injections are carried out after 3-4 months.

    Spasticity in the elbow joint area (flexion in the elbow joint)

    The average therapeutic dose of Lantox with a flexor in the elbow joint is 100-200 units. The total dose is distributed between the muscles: m. Biceps brachii - 50-100 ED, m.Brachialis - 25 units, m. Brachioradialis - 25 units. The injection is performed by the needles for intramuscular injections of 21 and 23G. EMG control is not required due to superficial muscle arrangement.

    Repeated injections are carried out after 3-4 months.

    Spasticity in the shoulder region (reduction of the shoulder and its internal rotation)

    During the injection the patient is in a sitting position. The average therapeutic dose of Lantox with shoulder reduction and its internal rotation is 150-250 units. The total dose is distributed between the muscles: w. Pectoralis major - 75 units, m. Teres major - 25 units, m. Subscapularis is 25 units and m. Latissimus dorsi - 25-50 units.

    Injections are performed with needles of size 21-23 G, EMG control is required. Repeated injections are carried out after 3-4 months.

    Spasticity of the muscles of the lower limb

    Spasticity in the foot (equinovarus deformation of the foot)

    The total dose of Lantox with equinovarus deformation of the foot is 200 units. If the drug is administered only in m. Gastrocnemius, then its dose is 100-150 units. The entire dose is distributed to the 2 head of the calf muscle and is inserted into 4 points (2 points per head). Injections are performed with a needle length of at least 4 cm. As a rule, EMG-control is not required. Injections are performed intramuscularly in the proximal quarter and distal 3/4 of the gastrocnemius muscle, or in the proximal 1/3 and distal 2/3 muscles.

    In those cases when the leading value in spasticity has an increased tone m. Soleus, the total dose of the drug administered is 50-100 units. In those cases when spasticity is caused by a high tone of both the gastrocnemius and soleus muscle, it is necessary to inject Lantox into both these muscles in a dose of 150-300 units.

    If the varus component dominates in the deformation of the foot, then it is necessary to carry out the combined introduction of Lantox as in m. Gastrocnemius in a dose of 100-150 ED, and in m. Tibialis posterior in a dose of 50-100 units. To maintain the effect, it is necessary to repeat injections, but not earlier than 2 months.

    The most commonly injected muscles are: m. Gastrocnemium, m. Soleus and Tibialis posterior (total dose 150 - 300 units).

    The average therapeutic dose for m. Gastrocnemius is 100-150 units. The total dose is distributed between the 2 heads of the gastrocnemius muscle and is introduced into 4 points (2 points per head). Injections are performed with a needle with a length of 23G. As a rule, EMG-control is not required.

    The average therapeutic dose for m. Soleus is 50-100 units. Injections are performed with a needle measuring 21G in length. As a rule, EMG-control is not required.

    The average therapeutic dose for Tibialis posterior is 50-100 units. EMG control is required. Repeated injections are carried out in 3-4 months.

    Spasticity in the knee region

    Equine deformity can be combined with spasticity of the posterior group of hip muscles leading to flexion contracture of the knee joint. In these cases, Lantox should be injected into the semitendinous and semimembranous muscles at a dose of 50-100 ED in 1-2 points of each muscle.

    Injections in m. Semitendinosus and m. Semimembranosus is performed by intramuscular needles of a size of 21 G, EMG monitoring is generally not required.

    If the spasticity of the quadriceps muscle dominates, an extension knee in the knee joint is formed. It is recommended that the drug is injected into the straight and lateral heads m. Quadriceps femoris in a total dose of 100-150 units.

    Injection into the rectum and lateral head m. Quadriceps femoris is performed with a needle 5-7 cm long, EMG monitoring is usually not necessary, because the muscles are superficially and well palpated. Repeated injections are carried out after 3-4 months. Spasticity in the hip area

    With spasticity in the proximal muscles of the femur - ilio-lumbar and rectus muscle of the thigh, Lantox is injected into m. Iliopsoas in a dose of 100-150 units. If necessary, additional injections into m can be made. Rectus femoris in a dose of 50-100 units.

    Injection into m.Iliopsoas perform a long needle - up to 10 cm, it is desirable to conduct EMG-control due to the deep arrangement of the muscle. The injection point is 3-4 cm lateral to the pulsation of the femoral artery, immediately below the inguinal ligament; depth of injection up to 7-8 cm. Repeated injections are carried out after 3-4 months.

    Hyperactive Bladder

    Produce endoscopic injection of the drug wall of the bladder under a constant visual control of 20-30 points per 1 ml at a rate of 10 units per 1 point of administration. The maximum dose of administration is 300 units.

    Detruzor-sphincter dissynergy

    External sphincter of the bladder (non-relaxing external sphincter of the urethra, detrusor-sphincter dissynergy)

    Lantox is administered transurethral or transperineal to the external urethral sphincter at a dose of 100 units under EMG control. The volume of the administered solution should not exceed 8 ml, and the dose of the injected drug should not exceed 100 units. Repeated injections are performed as needed, usually every 6-12 months.

    Sphincters of the rectum (paradoxical pu-rectal dissynergy, anal fissures, constipation)

    Lantox is injected into two points of each pu-rectal muscle in a total dose of 50-100 ED.To relax the internal anal sphincter, Lantox is injected into the anterior part of the sphincter under the control of EMG. The average dose is 20 units.

    With spasticity of perineal muscles, manifested by vaginismus, anemia, or anal fissure, the drug is administered transperineally.

    When vaginismus the drug is injected into the front wall of the vagina at a dose of 30-50 units.

    When anism (pathological spasm of the puborectal muscle) in a dose of 25-50 units per each puborectal muscle from both sides.

    When anal fissure Lantox injections are performed in the anterior part of the internal anal sphincter at a dose of 20 units.

    Repeated injections are performed as needed, usually every 6-12 months.

    Hyperfunctional facial wrinkles

    Forehead area

    Injections are made at a distance of 2-2.5 cm from the eyebrows. The injection points (usually 4-8 points) are located at an interval of 2 cm from each other. Injections are performed symmetrically, subcutaneously or intramuscularly, with the same dosage to avoid asymmetry of the eyebrows. The dose to each point is 2.0-4.0 units, the total dose: 8-32ED.

    Wrinkles in the bridge of the nose (between the eyebrows)

    If the patient has a deep and long inter-brow furrow, an additional 2.5-5.0 ED is administered at points located 5-7 mm above the primary points.The depth of needle insertion is 2-3 mm, the direction is vertical downwards.

    In addition, an additional injection is made to a point located in the center of the line connecting the medial edges of the eyebrows. The dose to this point is 2.5 to 7.5 units, depending on age and sex. Needle position - from front to back, depth of needle insertion - 2-3 mm. The total amount of the drug injected into the area between the eyebrows should not exceed 25 units.

    Wrinkles at the outer corners of the eyes

    Injections are administered subcutaneously in 2-4 points located 1.5 cm from the lateral angle of the eye, located symmetrically in the outer segment of the area, at a distance of 1-2 cm from each other, depending on the number of wrinkles in the patient. The dose to each point is 1.5-4 units, the total dose: 3-16 units per side.

    Wrinkles in the area of ​​the back of the nose

    In this area, injections are made at 2 points symmetrically in the region of the back of the nose intradermally. The dose to each point is 1.5-2 units, the total dose: 3.0-4.0 units.

    Along with the above-mentioned zones of Lantox administration, correction is sometimes required: above the upper lip to correct the vertical ("muscular") Lantox wrinkles (injected subcutaneously / intramuscularly into one point in the middle of the upper lip) or two points closer to the vermilion area, 5 mm from the red border of the lips; in the muscle, lowering the corners of the mouth (triangular muscle, m.Depressor anguli oris), to raise the corners of the mouth and reduce the severity of the lip-chin fold ("folds of sorrow"), Lantox is injected intradermally, at a distance of 1 cm from the edge of the lower jaw, to the projection point of the maximum activity of this muscle, at a dose of 2-3 units; for lifting the side facial (correction of the face oval) Lantox is injected subcutaneously in two points along the edge of the lower jaw at a distance of 2 cm from each other, at a dose of 2-3 units per point; in the field of the muscle of laughter to correct vertical wrinkles ("staples") lateral to the nasolabial fold Lantox is injected intradermically into 1-2 points located along the line of the corners of the mouth 2-3 cm lateral to the nasolabial fold; in the neck region for the correction of strands m. Platyzma Lantox is injected intramuscularly into the middle of each visible strand at a dose of 3-5 units per point.

    In these points Lantox is also administered in the presence of pathological syncopeies and contractures. To improve the relief of the anterior surface of the neck, Lantox is injected into an additional 4-6 points subcutaneously / intradermally at a dose of 1-2 units per point.

    Syncopeesis and contracture of facial muscles

    The injection points in the treatment of syncopeesis and contracture are identical to the points of hemifacial spasm, however, the dose of Lantox at each point and the total dose per procedure should be 25-50% lower.

    Strabismus

    In the treatment of strabismus, Lantox is injected with a coaxial electrode needle, electromyographic control under local anesthesia using 0.5% of dicain. Injections into the extraocular muscles are selected in accordance with the type of strabismus.

    For vertical and horizontal muscular strabismus with deviations less than 20 prism diopters, the initial dose to each muscle should be 1.25-2.5 units, for horizontal strabismus with deviations of 20-40 prisms diopters, the dose to each muscle is 2.5- 5 units, for horizontal strabismus with deviations 40-50 prisms diopters, the initial dose in each muscle is 2.5 units and can be increased (up to 5 units each time) depending on the effect. In the treatment of persistent paralysis of the cranial nerve VI, lasting more than 1 month, a dose of 1.25-2.5 units may be introduced into the medial rectus muscle.

    To create protective ptosis in patients with lagophthalmosis, Lantox is injected into the zone of the projection of the muscle lifting the upper eyelid in the middle of the upper eyelid intradermally, at a dose of 10-20 units.

    Vegetative disorders

    Hyperhidrosis

    The minimum dose is 0.5 units per 1 cm2, with intensive hyperhidrosis to 1-2 ED per 1 cm2. The recommended volume of the drug administered in one zone should not exceed 50 units.

    Injections are performed intradermally with an insulin syringe with non-removable needles measuring 29-33G.

    The distance between injection points is 1.5-2 cm, 2.0 units are injected into each point; the maximum dose for each point is 5.0 units (for areas with a particularly intense hyperhidrosis). The average dose for injection of one typical zone (palm, foot or armpit) in most cases is 50 units; the minimum dose is 30 units of Lantox. The average number of points for one typical zone is from 15 to 25.

    Repeated injections are carried out as needed, but not earlier than 2 months.

    Pain syndromes

    Myofascial pain syndromes

    Myofascial pain syndrome of the face. Myogenic painful dysfunction of the temporomandibular joint.

    Lantox is injected on the side of pain in the temporal muscles (10-30 units each), in the masticatory muscles (20-50 units each) and, if necessary, in the pterygoid muscles (10-40 units each). If bilateral injections are necessary, the total dose of the drug should be reduced.

    Upper chest aperture syndrome

    Lantox is introduced into the front staircase (in the central part) or into the small pectoral muscle into two trigger points (TT); in addition - in the TT of the large pectoral muscle. The total dose is 75-100 units.It is recommended simultaneous injection of 3-4 ml of local anesthetic.

    The needle is positioned perpendicular to the skin surface 3.8 cm above the clavicle (up to 2.5 cm above the collarbone there is a risk of injuring the pleura).

    Syndrome of shoulder-scapular periarthropathy

    Injections of Lantox in a total dose of 100-200 units are carried out in 2-5 most interested TT of the following muscles: supratenal, deltoid, subscapular, large round muscle. Possible simultaneous administration of up to 5 ml of local anesthetic.

    Mandatory injections in 2-3 TT of the supraspinous muscle, which are carried out with a needle 3-4 cm long. The medial TT is located above the spine of the scapula 2-3 cm outward from the medial margin; lateral TT - between the scapula and the clavicle at the medial edge of the acromion.

    "Tennis Elbow". Lantox in a dose of 20-40 units is injected under the EMG-control into the muscle of the common extensor of the fingers in combination with a local anesthetic.

    Pear-shaped muscle syndrome. Lantox is administered at a dose of 80-100 ED to the point located at the border of the lateral 1/3 line connecting the sacrum and the large spit; depth of injection up to 7 cm.

    With myofascial pain in the lumbar region, Lantox is injected into the pear-shaped, ilio-lumbar, square muscle of the waist with a dilution of 0.9% sodium chloride solution for injection. Simultaneously, the administration of an anesthetic is possible.It is advisable to inject under EMG control due to a deep muscle arrangement.

    The ilio-lumbar muscle: Lantox is administered at a dose of 100-150 ED to a point 3-4 cm lateral to the pulseless femoral artery, immediately below the inguinal ligament; depth of injection up to 7-8 cm.

    Square lumbar muscle: Lantox is administered at a dose of 100 units at 2-4 points corresponding to TT.

    Trism, bruxism. If the mouth is difficult to open, injections are done in three muscles (doses for one side are given): m. Temporalis - 20 units (10-50 units), t. Pterygoideus lateralis - 30 units (20-40 units), m. Masseter - 40 units (30-100 units). EMG control may be required. With a second injection, the dose of Lantox is usually 25% lower. It is permissible in cases of acute pain to inject Lantox solution together with 2 ml of a 2% solution of lidocaine.

    Chronic facial pain. When dislocation and dyslexia of the temporo-maxillary joint, Lantox should be inserted into both mm. Pterygoidei lateralis in a dose of 20 units on each side.

    Chronic headaches

    Treatment with Lantox is indicated for: severe migraine (more than 8 migraine attacks per month); chronic migraine; chronic tension headache with involvement of pericranial muscles; chronic daily headaches caused by a combination of different types of headaches (combined chronic headaches);tension of pericranial and cervical muscles; cervicogenic headaches; inefficiency of standard schemes of drug preventive therapy - as a "backup" therapy for chronic headaches. Each of the above indications individually is sufficient for the application of Lantox.

    Injections are produced in m. Procerus, bilateral in mm. Frontalis, Corrugator supercilii, Temporalis, Occipitalis. When performing injections in mm. Frontalis the lower points of the Lantox injection should be located 2 cm above the eyebrow line. In addition, mm is injected. Trapezius, Splenius capitis, Sternocleidomastoideus in cervicogenic and combined chronic headaches.

    Breeding Lantox - in 2.0 ml of a 0.9% solution of sodium chloride for injection at 100 units.

    Used insulin syringes with non-removable needles size 29-33G.

    The total dose of Lantox, equal to the sum of doses for all target muscles, is determined individually in each case. The dose depends on the type of headache, the severity of the patient's general condition, and the size of the injection areas (head or head and neck area).

    The number of injection points and dose values ​​are indicated in Table 2.

    Table 2. Doses of Lantox for injection into muscles in chronic headaches.

    Target muscles

    Average dose *

    (ED)

    Range of doses *

    (ED)

    amount

    points

    introduction *

    Frontal

    4

    3-10

    2-3

    Eyebrow Frown

    5

    4-15

    1-2

    Gordecov

    5

    4-8

    1-2

    The temporal

    15

    5-30

    2-4

    Occipital

    8

    5-20

    2-3

    Trapezoidal (rarely)

    25

    20-40

    2-4

    Belt head (rare)

    25

    20-40

    2-3

    Kivatelnaya (rarely)

    20

    15-30

    2-4

    * - doses and points for one side are presented. When calculating the total dose of injections, it is necessary to take into account the bilaterality of the drug administration.

    Injections are performed with insulin syringes with non-removable needles measuring 29-33G.

    Treatment, as a rule, begins with the use of the average dose recommended for the target muscle.

    The average total dose per procedure for one patient is 100 units, the maximum is 200 units.

    Clinical improvement in the form of an analgesic effect is observed at the end of the first month after the injection and persists for 3-6 months. If the effect of the first procedure is inadequate, repeated administration of Lantox in a larger dose after 3 months is recommended. To achieve a stable improvement, repeated injections are given once every 3-6 months.

    Dissolution of the preparation

    The preparation is dissolved with sterile isotonic sodium chloride solution for injection 0.9% in the required volume, according to the table.

    ED / 0.1 ml

    Number of units in the vial

    50

    100

    Volume of solvent (ml)

    10,0

    0,5

    1,0

    5,0

    1,0

    2,0

    2,5

    2,0

    4,0

    1,25

    4,0

    8,0

    When diluting the drug, it is forbidden to open the bottle, removing the stopper. Before diluting the contents of the vial, the central part of the rubber plug is treated with alcohol. For a puncture use a sterile needle size 23-25 G. The solvent should be injected through the wall, by means of light rotational movements of the vial the powder is mixed with the solvent for one minute. After the addition of the solvent, the vial is gently rocked until the drug dissolves completely. If the solvent is not drawn into the vial under the action of a vacuum, the vial is destroyed. The dissolved preparation should be transparent and colorless, without extraneous inclusions. The prepared injectable solution is injected with an insulin syringe, the size of the needle is determined by the size of the muscle and the depth of injection.

    The solution should be used immediately or stored in the cold at a temperature of 2 ° C to 8 ° C for no more than 4 hours. The container and syringe, as well as the remaining drug solution, are subject to destruction after sterilization. The dispensed product is to be neutralized with a solution of sodium hypochlorite.
    Side effects:

    In the treatment of blepharospasm and hemifacial spasm possibly the appearance of ptosis of the eyelid, reversal of the lower eyelid, slowing of the blinking frequency, incomplete closure of the eyelids, weakness of the facial muscles located in the immediate vicinity of the injection site. These symptoms disappear after 3-8 weeks without any treatment. The most likely and expected side effect after the injection is transient semiptosis, which can cause inconvenience for patients within 2-3 weeks. In these cases, you can recommend fixing the edge of the eyelid to the skin under the eyebrow.

    With endoscopic introduction of Lantox into the external sphincter of the urethra and detrusor possibly the emergence of transient incontinence of urine, hematuria and urethroragia, exacerbation of uroinfection. All complications are reversible and are usually eliminated by symptomatic treatment within 2-3 days.

    In the treatment chronic headaches there may be mild transient side effects - semiptosis, asymmetry of the eyebrows in the first 2 weeks, swelling of the upper eyelids. With excessive weakening of the muscles of the posterior parts of the head and the posterior-lateral group of the neck muscles, it is possible to break the extension of the neck.

    Typical side effect in the treatment hemifacial spasm - ptosis, develops as often as in the treatment of blepharospasm, especially if the drug is injected into the palpebral part of the circular muscle of the eye. More often ptosis occurs in patients with a lack of function of the facial nerve.

    Side effects in the treatment of hyperhidrosis minimal (1-2%): local microhematomas and slight transient weakness of small muscles of the hand or fingers when injecting this area.

    In the treatment spasticity the most common side effects are flu-like symptoms, dry mouth, pain at the injection site, pharyngitis, general weakness, constipation, diarrhea, drowsiness. As a rule, these side effects disappear within two weeks and do not require separate treatment.

    "Tennis Elbow". When injected into the common extensor of the fingers, some patients develop a weakness of extension of the fingers of the hand.

    When treating strabismus in some patients, temporary ptosis of a different degree can occur, vertical deviations and, very rarely, mydriasis, due to the spread of toxin to adjacent muscles. These symptoms disappear within a few weeks without any treatment.

    The doctor should warn the patient about the possibility of developing these side effects and the need for timely seeking medical help.

    Interaction:The action of Lantox can be enhanced with antibiotics-aminoglycosides (eg, gentamycin). In connection with this, these drugs are not used together with Lantox.
    Special instructions:

    Precautionary measures:

    1. A specially appointed person must be responsible for storage, leave and registration of the drug. The drug is prescribed only for the treatment of patients who have the above indications. Before starting to use Lantox in treating strabismus, the doctor must undergo special training, know the anatomy of the muscles well, and also know the technique of using electromyographic injection control.

    2. Patients suffering from chronic diseases (heart, liver, lungs, blood, acute form of tuberculosis) should begin treatment with the drug with the minimum recommended dose.

    3. The room where Lantox is administered should be provided with anti-shock therapy, including adrenaline 1: 1000.

    4.Lantox is stored in a separate closed labeled box in the refrigerator of the medical institution where the injections of the drug are carried out. The drug can not be given to the patient for storage.

    Form release / dosage:Liofilizate for the preparation of solution for injection, 50 units and 100 units.
    Packaging:

    In the vial.

    1 bottle in a blister pack in a cardboard box pack with instructions for use.

    Storage conditions:

    Store at temperatures from minus 5 ° C to minus 20 ° C, out of the reach of children.

    Transport at a temperature of minus 5 ° C to minus 20 ° C.

    Shelf life:

    3 years.

    The drug with expired shelf life is not subject to application.
    Terms of leave from pharmacies:For hospitals
    Registration number:LSR-001587/08
    Date of registration:14.03.2008 / 22.06.2009
    Expiration Date:Unlimited
    The owner of the registration certificate:NIKE-MED, LLC NIKE-MED, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp15.02.2018
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